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Cre 8 It, Inc. Recall: Stuffing Mix was recalled after receiving a complaint of sour taste. Firm determined storage trailer thermometer was 4 degrees off.

United States

TerminatedClass II

Company
Cre 8 It, Inc.
Product
Cre 8 It, Inc. Stuffing, 011951311916 in covered aluminum fo…
Recall date
November 18, 2016
Terminated
April 24, 2018
Source
FDA

Reason for recall

Stuffing Mix was recalled after receiving a complaint of sour taste. Firm determined storage trailer thermometer was 4 degrees off.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Cre 8 It, Inc. Stuffing, 011951311916 in covered aluminum foil pans. Net Weight 2/4 lb. (3.63kg) containers per shipping case Not published in this source record 683 cases Expiration dates of 12/4, 12/7, 12/9, 12/11,12/14

Distribution

  • MN

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0615-2017
Event ID
75759
Status
Terminated
Classification
Class II
Company
Cre 8 It, Inc.
Product description
Cre 8 It, Inc. Stuffing, 011951311916 in covered aluminum foil pans. Net Weight 2/4 lb. (3.63kg) containers per shipping case
Quantity
683 cases
Reason
Stuffing Mix was recalled after receiving a complaint of sour taste. Firm determined storage trailer thermometer was 4 degrees off.
Recall initiation date
November 18, 2016
Report date
December 14, 2016
Classification date
Not published in this source record
Termination date
April 24, 2018
Distribution pattern
MN
UPC, lot, and code information
Expiration dates of 12/4, 12/7, 12/9, 12/11,12/14
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Cre 8 It, Inc.

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Minnesota 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

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